HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030688Generated: October 26, 2026
Chloromethyl Methyl Ether → 2-Methoxy-1-phenylethanone
https://huagongshe.com/reaction/1030688
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | 2',4',6'-Trihydroxyacetophenone | HCID 68073 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methoxy-1-phenylethanone | HCID 77698 | — |
Reaction Steps
In 200 ml of anhydrous tetrahydrofuran were dissolved 30 g of 2',4',6'-trihydroxyacetophenone and 115.0 g of N,N-diisopropylethylamine, and 50.2 g of chloromethyl methyl ether was gradually added to the solution under ice cooling over a period of 20 minutes and the reaction mixture was stirred under ice cooling for 1 hour and at room temperature for 4 hours to effect reaction. After the reaction, the reaction mixture was extracted with 3 l of ether, and the ether layer was washed with water (500 ml×3 times), shaken with a saturated aqueous solution of sodium chloride (300 ml×2 times), dried with anhydrous sodium sulfate, and filtered. The solvent was removed from the filtrate by distillation and the obtained residue was recrystallized from a mixed solvent of methanol and water to obtain 18.9 g (yield=41.4%) of 2'-hydroxy-4',6'-bis(methoxyacetophenone in the form of a colorless prism.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05106871 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-67ac17e98d9249d1acf9eb381098a0d1 |
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| Source note | uspto-grants-1992_04 |
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